Title : Methionine auxotrophy in inborn errors of cobalamin metabolism.

Pub. Date : 1992 Aug

PMID : 1516297






2 Functional Relationships(s)
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1 Several of the inborn errors of vitamin B12 (cobalamin, Cbl) metabolism (cblC, cblD, cblE, cblF, cblG) are associated with homocystinuria and hypomethioninemia due to a functional deficiency of the cytoplasmic enzyme methionine synthase which requires methylcobalamin (MeCbl) as a cofactor. mecobalamin Cbl proto-oncogene Homo sapiens
2 Several of the inborn errors of vitamin B12 (cobalamin, Cbl) metabolism (cblC, cblD, cblE, cblF, cblG) are associated with homocystinuria and hypomethioninemia due to a functional deficiency of the cytoplasmic enzyme methionine synthase which requires methylcobalamin (MeCbl) as a cofactor. mecobalamin Cbl proto-oncogene Homo sapiens